SVA: software for annotating and visualizing sequenced human genomes (Q34188360)

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English	SVA: software for annotating and visualizing sequenced human genomes	scientific article

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scholarly article

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Europe PubMed Central

PubMed publication ID

21624899

retrieved

31 July 2017

title

SVA: software for annotating and visualizing sequenced human genomes (English)

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Europe PubMed Central

PubMed publication ID

21624899

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31 July 2017

main subject

visualization

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based on heuristic

inferred from title

software

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author

Anna C. Need

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7

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Europe PubMed Central

PubMed publication ID

21624899

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31 July 2017

Elizabeth T Cirulli

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8

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Europe PubMed Central

PubMed publication ID

21624899

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31 July 2017

Kevin V Shianna

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3

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Kevin V Shianna

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Europe PubMed Central

PubMed publication ID

21624899

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31 July 2017

Erin L Heinzen

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6

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Erin L Heinzen

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Europe PubMed Central

PubMed publication ID

21624899

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31 July 2017

David B. Goldstein

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14

object named as

David B Goldstein

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Europe PubMed Central

PubMed publication ID

21624899

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31 July 2017

Dongliang Ge

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1

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Dongliang Ge

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Europe PubMed Central

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21624899

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31 July 2017

Jessica M Maia

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9

object named as

Jessica M Maia

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PubMed publication ID

21624899

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31 July 2017

author name string

Elizabeth K Ruzzo

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2

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Europe PubMed Central

PubMed publication ID

21624899

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31 July 2017

Min He

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4

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PubMed publication ID

21624899

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31 July 2017

Kimberly Pelak

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5

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Europe PubMed Central

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21624899

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31 July 2017

Samuel P Dickson

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10

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Europe PubMed Central

PubMed publication ID

21624899

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31 July 2017

Mingfu Zhu

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11

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Europe PubMed Central

PubMed publication ID

21624899

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31 July 2017

Abanish Singh

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12

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Europe PubMed Central

PubMed publication ID

21624899

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31 July 2017

Andrew S Allen

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13

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Europe PubMed Central

PubMed publication ID

21624899

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31 July 2017

language of work or name

English

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publication date

29 May 2011

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Europe PubMed Central

PubMed publication ID

21624899

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31 July 2017

published in

Bioinformatics

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Europe PubMed Central

PubMed publication ID

21624899

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31 July 2017

volume

27

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Europe PubMed Central

PubMed publication ID

21624899

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31 July 2017

issue

14

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Europe PubMed Central

PubMed publication ID

21624899

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31 July 2017

page(s)

1998-2000

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Europe PubMed Central

PubMed publication ID

21624899

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31 July 2017

copyright license

Creative Commons Attribution-NonCommercial 2.5 Generic

start time

2 October 2016

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April 2023 Public Data File from Crossref

copyright status

copyrighted

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cites work

Integrative genomics viewer

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129530

retrieved

5 July 2018

A map of human genome variation from population-scale sequencing

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129530

retrieved

5 July 2018

The characterization of twenty sequenced human genomes

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stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129530

retrieved

5 July 2018

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129530

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5 July 2018

Whole-genome sequencing of a single proband together with linkage analysis identifies a Mendelian disease gene

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129530

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5 July 2018

Savant: genome browser for high-throughput sequencing data

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129530

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5 July 2018

Whole-genome sequencing in a patient with Charcot-Marie-Tooth neuropathy

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129530

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5 July 2018

Analysis of genetic inheritance in a family quartet by whole-genome sequencing

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129530

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5 July 2018

Exome sequencing identifies the cause of a mendelian disorder

1 reference

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129530

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5 July 2018

Ensembl's 10th year

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129530

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5 July 2018

KEGG for representation and analysis of molecular networks involving diseases and drugs

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129530

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5 July 2018

Genetic diagnosis by whole exome capture and massively parallel DNA sequencing

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129530

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5 July 2018

BreakDancer: an algorithm for high-resolution mapping of genomic structural variation

1 reference

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129530

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5 July 2018

The Sequence Alignment/Map format and SAMtools

1 reference

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129530

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5 July 2018

Fast and accurate short read alignment with Burrows-Wheeler transform

1 reference

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129530

retrieved

5 July 2018

Combinatorial algorithms for structural variation detection in high-throughput sequenced genomes

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129530

retrieved

5 July 2018

Ultrafast and memory-efficient alignment of short DNA sequences to the human genome

1 reference

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129530

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5 July 2018

Accurate whole human genome sequencing using reversible terminator chemistry

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129530

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5 July 2018

Genome-wide association studies for complex traits: consensus, uncertainty and challenges

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129530

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5 July 2018

WGAViewer: software for genomic annotation of whole genome association studies

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129530

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5 July 2018

A second generation human haplotype map of over 3.1 million SNPs

1 reference

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129530

retrieved

5 July 2018

Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129530

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5 July 2018

NCBI reference sequences (RefSeq): a curated non-redundant sequence database of genomes, transcripts and proteins

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129530

retrieved

5 July 2018

Detection of large-scale variation in the human genome

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129530

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5 July 2018

Gene ontology: tool for the unification of biology

1 reference

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129530

retrieved

5 July 2018

Identifiers

DOI

10.1093/BIOINFORMATICS/BTR317

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stated in

Europe PubMed Central

PubMed publication ID

21624899

retrieved

31 July 2017

DBLP publication ID

journals/bioinformatics/GeRSHPHNCMDZSAG11

1 reference

stated in

DBLP Dataset 2021-01-02

retrieved

28 January 2021

PMC publication ID

3129530

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21624899

retrieved

31 July 2017

PubMed publication ID

21624899

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21624899

retrieved

31 July 2017

ResearchGate publication ID

51176979

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